1-(2-Hydroxypropyl)-4-(4-methoxyphenyl)-3-phenoxyazetidin-2-one

Base Information

Chemical Name:1-(2-Hydroxypropyl)-4-(4-methoxyphenyl)-3-phenoxyazetidin-2-one
CAS No.:111821-17-1
Molecular Formula:C19H21NO4
Molecular Weight:327.38
Hs Code.:
DSSTox Substance ID:DTXSID00549242
Mol file:111821-17-1.mol

Synonyms:111821-17-1;1-(2-Hydroxypropyl)-4-(4-methoxyphenyl)-3-phenoxyazetidin-2-one;DTXSID00549242

Suppliers and Price of 1-(2-Hydroxypropyl)-4-(4-methoxyphenyl)-3-phenoxyazetidin-2-one

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1-(2-Hydroxypropyl)-4-(4-methoxyphenyl)-3-phenoxyazetidin-2-one

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:327.14705815
Heavy Atom Count:24
Complexity:416

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(CN1C(C(C1=O)OC2=CC=CC=C2)C3=CC=C(C=C3)OC)O

Technology Process of 1-(2-Hydroxypropyl)-4-(4-methoxyphenyl)-3-phenoxyazetidin-2-one

There total 4 articles about 1-(2-Hydroxypropyl)-4-(4-methoxyphenyl)-3-phenoxyazetidin-2-one which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 111761-78-5
N-(4-methoxybenzylidene)-2-trimethylsiloxypropylamine

: 122-59-8
2-phenoxyacetic acid

: 111761-80-9,111821-17-1,111821-19-3
cis-1-(2-hydroxypropyl)-3-phenoxy-4-(p-methoxyphenyl)azetidin-2-one

Guidance literature:: With O-phenyl phosphorodichloridate; triethylamine; In dichloromethane; at 0 ℃; Yield given;

Reference yield:

: 111761-78-5
[1-(4-Methoxy-phenyl)-meth-(E)-ylidene]-(2-trimethylsilanyloxy-propyl)-amine

: 122-59-8
2-phenoxyacetic acid

: 111761-80-9,111821-17-1,111821-19-3
cis-1-(2-hydroxypropyl)-3-phenoxy-4-(p-methoxyphenyl)azetidin-2-one

Guidance literature:: With O-phenyl phosphorodichloridate; triethylamine; In dichloromethane;
DOI:10.1016/S0040-4020(01)81678-1

Reference yield:

: 123-11-5
4-methoxy-benzaldehyde

: 111761-80-9,111821-17-1,111821-19-3
cis-1-(2-hydroxypropyl)-3-phenoxy-4-(p-methoxyphenyl)azetidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: 2.) triethylamine / 1.) methylene dichloride, room temp.; 2.) methylene dichloride, 0 deg C, 60 min

2: 2.) aq HCl / 1.) methylene dichloride, room temp., 20 to 24 h; 2.) acetone, room temp., 30 min

With hydrogenchloride; triethylamine;